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Part Time Biotech Quality Control Jobs (NOW HIRING)

Antheia

Senior Quality Control Manager

Menlo Park, CA · On-site

$160K - $195K/yr

We're looking for a Senior QC Manager to own quality control across our GMP and non-GMP ... Part-time ( temporary roles are not eligible for Company sponsored benefits. * Comprehensive ...

SANS Institute

PT Quality Control Analyst

Bethesda, MD · On-site +1

$26 - $30/hr

What You'll Achieve at SANS We are seeking a Quality Control Analyst to join our Courseware ... Work Schedule * Part-time, less than 30 hours per week * Typical schedule is Monday-Thursday, 8:00 ...

Metromont LLC

QC Lab Technician

Hiram, GA · On-site

$17.25 - $22/hr

QUALITY CONTROL SUPERVISOR(S): TERRY SNOW REVIEW DATE : 02/19/09 * Climbing: n/a * Repetitive ... P, Electrical Safety awareness, Forklift certification, Haz Com, Overhead Crain Training, P.T. , ...

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Part Time Biotech Quality Control information

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How much do part time biotech quality control jobs pay per hour?

As of Jul 11, 2026, the average hourly pay for part time biotech quality control in the United States is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

What are some common challenges faced by part-time professionals in Biotech Quality Control, and how can they effectively manage them?

Part-time Biotech Quality Control professionals often face challenges such as staying up-to-date with evolving protocols, maintaining consistency in quality documentation, and ensuring seamless communication with full-time staff. To manage these, it's important to maintain organized records, proactively schedule regular check-ins with team members, and leverage digital tools for real-time updates on projects. Additionally, building strong relationships with colleagues ensures better knowledge transfer and team cohesion, which helps maintain high-quality standards even with a part-time schedule.

What are part-time biotech quality control jobs?

Part-time biotech quality control jobs involve ensuring that biotechnology products or processes meet established quality standards, but on a reduced or flexible schedule. These roles typically include tasks like testing samples, documenting results, and identifying deviations from quality guidelines. Part-time positions are ideal for students, professionals seeking work-life balance, or those looking to gain experience in the biotech industry without committing to full-time hours. Employers may require relevant education or laboratory experience, depending on the complexity of the role.

What are the key skills and qualifications needed to thrive as a Part Time Biotech Quality Control professional, and why are they important?

To thrive as a Part Time Biotech Quality Control professional, you need a strong background in biology or chemistry, attention to detail, and familiarity with industry quality standards, often supported by a relevant degree or laboratory experience. Proficiency with laboratory instruments, data analysis software, and understanding of Good Manufacturing Practices (GMP) or ISO standards is typically required. Strong organizational skills, effective communication, and the ability to work independently are standout soft skills in this role. These competencies ensure accurate product testing, compliance with regulations, and contribute to the overall safety and success of biotech operations.

What is the difference between Part Time Biotech Quality Control vs Part Time Biotech Laboratory Technician?

AspectPart Time Biotech Quality ControlPart Time Biotech Laboratory Technician
CredentialsTypically requires a degree in biology, chemistry, or related fieldUsually requires a similar degree, sometimes with additional certifications
Work EnvironmentQuality control labs, manufacturing facilitiesResearch labs, testing facilities
Employer & Industry UsageBiotech, pharmaceutical companies, manufacturingResearch institutions, biotech firms, pharmaceutical companies
Common Search & Comparison IntentUnderstanding roles in quality assuranceUnderstanding lab testing and research roles

Part Time Biotech Quality Control focuses on ensuring products meet quality standards through testing and inspection, often in manufacturing settings. In contrast, Part Time Biotech Laboratory Technicians support research and testing activities, assisting in experiments and data collection. Both roles require similar educational backgrounds but differ in daily tasks and work environments.

More about Part Time Biotech Quality Control jobs
What cities are hiring for Part Time Biotech Quality Control jobs? Cities with the most Part Time Biotech Quality Control job openings:
What are the most commonly searched types of Biotech Quality Control jobs? The most popular types of Biotech Quality Control jobs are:
What states have the most Part Time Biotech Quality Control jobs? States with the most job openings for Part Time Biotech Quality Control jobs include:
What job categories do people searching Part Time Biotech Quality Control jobs look for? The top searched job categories for Part Time Biotech Quality Control jobs are:
Part Time Biotech Quality Control jobs near you
Infographic showing various Part Time Biotech Quality Control job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 91% Full Time, 1% Part Time, 1% Temporary, and 5% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $44,668 per year, or $21.5 per hour.
Senior Quality Control Manager

Senior Quality Control Manager

Antheia

Menlo Park, CA • On-site

$160K - $195K/yr

Full-time, Part-time

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago

Job description

About Antheia:
Antheia is the advanced biosynthesis company transforming pharmaceutical manufacturing and innovation for the 21st century. Antheia's commercially proven technology platform produces high-value pharmaceutical ingredients in a fraction of the time compared to legacy approaches while significantly reducing supply chain risk. The company provides its global pharmaceutical customers with a resilient, efficient supply of critical ingredients at scale, while expanding the innovation frontier for new therapeutic development. Backed by leading investors and recognized by the U.S. government as a priority technology for public health and national and economic security, Antheia is manufacturing the medicines the world needs today while enabling tomorrow's breakthrough therapeutics.
Working at Antheia:
Our cross-functional team shares a vision for the future: improved pharmaceutical supply chains that can end drug shortages and drive equitable access to essential medicines. As a team, we aim to embody a culture that celebrates diversity, prioritizes knowledge sharing, encourages exploration and ideation, challenges constructively, and supports individuals in their professional and personal journeys. At Antheia, you can expect to be inspired by the science, by your teammates, and by the opportunity we have to bring about change in the pharmaceutical industry.
We're looking for a Senior QC Manager to own quality control across our GMP and non-GMP environments, from R&D through commercial manufacturing. You'd lead a team of QC Analysts and Specialists, serve as the primary interface with our CDMO and contract lab partners, and build the systems and processes that scale with us as we grow.
What You'll Own
Team & Operations
  • Lead and develop a team of QC Analysts and Specialists: hiring, mentoring, performance, day-to-day priorities
  • Build and improve lab operations infrastructure (scheduling, resource planning, data review workflows)
  • Ensure compliance with GMP, ICH, USP/EP, and FDA/EMA standards across all applicable testing

External Partnerships
  • Serve as the primary QC point of contact for CDMOs, CROs, and contract testing labs
  • Review and approve analytical packages, protocols, and reports from third parties for regulatory compliance and data integrity
  • Drive resolution when external partners hit analytical issues or timeline delays

Technical Leadership
  • Lead method development, transfer, and validation aligned with ICH Q2(R2) and Q14
  • Own complex investigations (OOS, OOT) through root cause analysis and CAPA, with a bias toward speed and continuous improvement
  • Ensure data integrity across workflows (ALCOA+ principles, LIMS, Empower, ELNs)

Strategy
    • Develop QC strategies that align with product lifecycle and multi-site growth
    • Contribute to vendor selection, lab qualification, and capital planning
    • Support regulatory filings with accurate, complete analytical documentation

Qualifications
  • Bachelor's or Master's degree in Chemistry, Biology, or related field. Advanced degree preferred.
  • 10+ years of progressive experience in pharmaceutical QC under GMP regulations, with 5+ years in a leadership or managerial role.
  • Demonstrated experience managing QC laboratories, supervising analytical staff, and coordinating external testing activities.
  • Deep knowledge of chromatographic (HPLC, GC), spectroscopic (UV/Vis, FTIR), and wet chemistry techniques; bioanalytical familiarity is a plus.
  • Strong background in method development, validation, and lifecycle management (ICH Q2, Q14).
  • Solid experience in OOS/OOT investigations, deviation handling, and CAPA implementation.
  • In-depth understanding of FDA, EMA, and ICH regulatory expectations; prior audit experience highly desirable.
  • Familiarity with laboratory systems such as LIMS, Empower, and ELNs.
  • Excellent written and verbal communication skills with ability to lead cross-functional teams and interface with regulatory agencies and partners.

Additional Information:
  • Base salary: $160,000 - $195,000 + annual bonus + equity in a high-growth company

[1] This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice.
Please note that Antheia doesn't discriminate based on age, race, ethnicity, national origin, religion, gender, sexual orientation, disability, medical history, and other non-merit characteristics.
For full-time employees, Antheia offers a comprehensive total rewards package. Part-time (<30 hours per week) and temporary roles are not eligible for Company sponsored benefits.
  • Comprehensive compensation package, which includes annual bonus potential and equity opportunities
  • Paid time off, in addition to company-observed holidays
  • Excellent medical, dental, and vision insurance
  • 401(k) retirement savings plan
  • Free access to the Menlo Park Labs Gym
  • Menlo Park Labs free shuttle service to CalTrain, BART Station, and SF

Antheia is an equal opportunity employer and does not discriminate based on race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical conditions, veteran status, sexual orientation, gender (including gender identity and gender expression), taking or requesting statutorily protected leave, or any other basis protected by law. In addition, Antheia prohibits the harassment of any individual on any of the bases listed above or any other characteristics protected under federal, state, or local laws.
Legal authorization to work in the United States is required. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire..

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